Einträge von Griese, M. auf dem Publikationsserver

Winter, J., Essmann, S., Kidszun, A., Aslanidis, C., Griese, M., Poplawska, K., Bartsch, M., Schmitz, G. und Mildenberger, E. (2014) Neonatal Respiratory Insufficiency Caused by an (Homozygous) ABCA3-Stop Mutation: a Systematic Evaluation of Therapeutic Options. Klinische Pädiatrie 226 (02), S. 53-58. Volltext nicht vorhanden.

Kleinlein, B., Griese, M., Liebisch, Gerhard , Krude, H., Lohse, Peter, Aslanidis, Charalampos, Schmitz, Gerd, make_name_string expected hash reference und make_name_string expected hash reference (2011) Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis. Archives of Disease in Childhood / Fetal and Neonatal 96, F453-F456.